Titin and desmosomal genes in the natural history of arrhythmogenic right ventricular cardiomyopathy - Wikidata - wikimedia - TriplyDB

Titin and desmosomal genes in the natural history of arrhythmogenic right ventricular cardiomyopathy

Titin and desmosomal genes in the natural history of arrhythmogenic right ventricular cardiomyopathy

http://www.wikidata.org/entity/Q28246696

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A Review of the Giant Protein Titin in Clinical Molecular Diagnostics of Cardiomyopathies Rare coding TTN variants are associated with electrocardiographic QT interval in the general population Genotype-phenotype relationship in patients with arrhythmogenic right ventricular cardiomyopathy caused by desmosomal gene mutations: A systematic review and meta-analysis.Rare Titin (TTN) Variants in Diseases Associated with Sudden Cardiac Death Recent Advances in Understanding and Managing Cardiomyopathy.Genetic analysis of sick sinus syndrome in a family harboring compound CACNA1C and TTN mutations.

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Titin and desmosomal genes in the natural history of arrhythmogenic right ventricular cardiomyopathy

http://www.wikidata.org/entity/Q28246696

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2014 nî lūn-bûn

@nan

2014 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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JMEDGENET-2014-102591

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Journal of Medical Genetics

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Titin and desmosomal genes in ...... ght ventricular cardiomyopathy

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Anita Spezzacatene

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Bruno Pinamonti

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Carl V Barnes

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Dobromir Slavov

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Ernesto E Salcedo

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Francesca Brun

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Gianfranco Sinagra

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Giulia Barbati

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Luisa Mestroni

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Marco Merlo

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P2860

Titin-based tension in the cardiac sarcomere: molecular origin and physiological adaptations

A method and server for predicting damaging missense mutations

Arrhythmogenic right ventricular dysplasia/cardiomyopathy: pathogenic desmosome mutations in index-patients predict outcome of family screening: Dutch arrhythmogenic right ventricular dysplasia/cardiomyopathy genotype-phenotype follow-up study

Arrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in the desmosomal gene desmocollin-2

Comprehensive desmosome mutation analysis in north americans with arrhythmogenic right ventricular dysplasia/cardiomyopathy

Desmosomal gene analysis in arrhythmogenic right ventricular dysplasia/cardiomyopathy: spectrum of mutations and clinical impact in practice

Plakophilin-2 mutations are the major determinant of familial arrhythmogenic right ventricular dysplasia/cardiomyopathy

Guidelines for investigating causality of sequence variants in human disease

Human non-synonymous SNPs: server and survey

Single molecule force spectroscopy on titin implicates immunoglobulin domain stability as a cardiac disease mechanism.

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